Clinical Data Programmer I

At Clario, a part of Thermo Fisher Scientific, we are transforming clinical trials through innovative data solutions that improve patient outcomes. As a Clinical Data Programmer I, you will support the development, validation, and delivery of clinical datasets, working closely with cross-functional teams to ensure high-quality, compliant data outputs across studies. What We Offer Competitive compensation and benefits package Flexible remote working environment Opportunities for career growth and exposure to multiple clinical modalities A collaborative, global team focused on advancing clinical research What You’ll Be Doing Develop and test SAS and/or Python programs to generate standard and non-standard clinical data files Review and interpret data specifications, collaborating with Data Management to finalize requirements Support the validation of encoding and programming outputs to ensure accuracy and compliance Process data extracts and manage daily encoding requests to support ongoing study activities Contribute to study archival processes and ensure data deliverables meet project timelines Perform ad-hoc programming and data analysis activities, including quality control checks, data mining, and custom client requests Participate in client meetings, as appropriate, to understand data collection and reporting requirements Create and/or review functional and technical specifications based on user requirements Partner with Data Management to support data review and issue resolution activities Contribute to process improvements, SOP development, and documentation related to Clinical Data Programming Assist with onboarding and training of team members, as needed What We Look For Bachelor’s degree in Life Sciences, Computer Science, or a related field preferred SAS Base certification required Experience developing programs using advanced SAS procedures; exposure to Python is beneficial Understanding of database design, data structures, and clinical data workflows Familiarity with the pharmaceutical drug development process Experience working with CDISC SDTM standards and domains (e.g., EG, CO, DM, RE, VS, SUPP) Strong analytical, problem-solving, and organizational skills High attention to detail with a commitment to data quality Effective written and verbal communication skills Proficiency with Microsoft Office tools Fluency in English (spoken and written) At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster. Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.